Classifications

• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
  • C03C25/10—Coating
  • C03C25/24—Coatings containing organic materials
  • C03C25/26—Macromolecular compounds or prepolymers
  • C03C25/28—Macromolecular compounds or prepolymers obtained by reactions involving only carbon-to-carbon unsaturated bonds
  • C03C25/285—Acrylic resins
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
  • C09D175/04—Polyurethanes
  • C09D175/14—Polyurethanes having carbon-to-carbon unsaturated bonds
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C13/00—Fibre or filament compositions
  • C03C13/04—Fibre optics, e.g. core and clad fibre compositions
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
  • C03C25/10—Coating
  • C03C25/104—Coating to obtain optical fibres
  • C03C25/106—Single coatings
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
  • C03C25/10—Coating
  • C03C25/24—Coatings containing organic materials
  • C03C25/25—Non-macromolecular compounds
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
  • C03C25/10—Coating
  • C03C25/24—Coatings containing organic materials
  • C03C25/26—Macromolecular compounds or prepolymers
  • C03C25/32—Macromolecular compounds or prepolymers obtained otherwise than by reactions involving only carbon-to-carbon unsaturated bonds
  • C03C25/326—Polyureas; Polyurethanes
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C25/00—Surface treatment of fibres or filaments made from glass, minerals or slags
  • C03C25/10—Coating
  • C03C25/24—Coatings containing organic materials
  • C03C25/40—Organo-silicon compounds
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/08—Processes
  • C08G18/10—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step
  • C08G18/12—Prepolymer processes involving reaction of isocyanates or isothiocyanates with compounds having active hydrogen in a first reaction step using two or more compounds having active hydrogen in the first polymerisation step
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/30—Low-molecular-weight compounds
  • C08G18/36—Hydroxylated esters of higher fatty acids
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/40—High-molecular-weight compounds
  • C08G18/48—Polyethers
  • C08G18/4825—Polyethers containing two hydroxy groups
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/65—Low-molecular-weight compounds having active hydrogen with high-molecular-weight compounds having active hydrogen
  • C08G18/66—Compounds of groups C08G18/42, C08G18/48, or C08G18/52
  • C08G18/6629—Compounds of groups C08G18/42, C08G18/48, or C08G18/52 with compounds of group C08G18/36 or hydroxylated esters of higher fatty acids of C08G18/38
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/28—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the compounds used containing active hydrogen
  • C08G18/67—Unsaturated compounds having active hydrogen
  • C08G18/675—Low-molecular-weight compounds
  • C08G18/6755—Unsaturated carboxylic acids
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08G—MACROMOLECULAR COMPOUNDS OBTAINED OTHERWISE THAN BY REACTIONS ONLY INVOLVING UNSATURATED CARBON-TO-CARBON BONDS
  • C08G18/00—Polymeric products of isocyanates or isothiocyanates
  • C08G18/06—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen
  • C08G18/70—Polymeric products of isocyanates or isothiocyanates with compounds having active hydrogen characterised by the isocyanates or isothiocyanates used
  • C08G18/72—Polyisocyanates or polyisothiocyanates
  • C08G18/74—Polyisocyanates or polyisothiocyanates cyclic
  • C08G18/75—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic
  • C08G18/758—Polyisocyanates or polyisothiocyanates cyclic cycloaliphatic containing two or more cycloaliphatic rings
• • C—CHEMISTRY; METALLURGY
  • C08—ORGANIC MACROMOLECULAR COMPOUNDS; THEIR PREPARATION OR CHEMICAL WORKING-UP; COMPOSITIONS BASED THEREON
  • C08K—Use of inorganic or non-macromolecular organic substances as compounding ingredients
  • C08K5/00—Use of organic ingredients
  • C08K5/54—Silicon-containing compounds
  • C08K5/548—Silicon-containing compounds containing sulfur
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D133/00—Coating compositions based on homopolymers or copolymers of compounds having one or more unsaturated aliphatic radicals, each having only one carbon-to-carbon double bond, and at least one being terminated by only one carboxyl radical, or of salts, anhydrides, esters, amides, imides, or nitriles thereof; Coating compositions based on derivatives of such polymers
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D175/00—Coating compositions based on polyureas or polyurethanes; Coating compositions based on derivatives of such polymers
  • C09D175/04—Polyurethanes
  • C09D175/08—Polyurethanes from polyethers
• • C—CHEMISTRY; METALLURGY
  • C09—DYES; PAINTS; POLISHES; NATURAL RESINS; ADHESIVES; COMPOSITIONS NOT OTHERWISE PROVIDED FOR; APPLICATIONS OF MATERIALS NOT OTHERWISE PROVIDED FOR
  • C09D—COATING COMPOSITIONS, e.g. PAINTS, VARNISHES OR LACQUERS; FILLING PASTES; CHEMICAL PAINT OR INK REMOVERS; INKS; CORRECTING FLUIDS; WOODSTAINS; PASTES OR SOLIDS FOR COLOURING OR PRINTING; USE OF MATERIALS THEREFOR
  • C09D7/00—Features of coating compositions, not provided for in group C09D5/00; Processes for incorporating ingredients in coating compositions
  • C09D7/40—Additives
  • C09D7/60—Additives non-macromolecular
  • C09D7/63—Additives non-macromolecular organic
• • G—PHYSICS
  • G02—OPTICS
  • G02B—OPTICAL ELEMENTS, SYSTEMS OR APPARATUS
  • G02B6/00—Light guides; Structural details of arrangements comprising light guides and other optical elements, e.g. couplings
  • G02B6/02—Optical fibres with cladding with or without a coating
  • G02B6/02395—Glass optical fibre with a protective coating, e.g. two layer polymer coating deposited directly on a silica cladding surface during fibre manufacture
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C2213/00—Glass fibres or filaments
• • C—CHEMISTRY; METALLURGY
  • C03—GLASS; MINERAL OR SLAG WOOL
  • C03C—CHEMICAL COMPOSITION OF GLASSES, GLAZES OR VITREOUS ENAMELS; SURFACE TREATMENT OF GLASS; SURFACE TREATMENT OF FIBRES OR FILAMENTS MADE FROM GLASS, MINERALS OR SLAGS; JOINING GLASS TO GLASS OR OTHER MATERIALS
  • C03C2217/00—Coatings on glass
  • C03C2217/20—Materials for coating a single layer on glass
  • C03C2217/29—Mixtures

Definitions

• This disclosure pertains to fiber coatings with good strippability for splicing. More particularly, this disclosure pertains to primary fiber coatings with low pullout force and strong cohesion.
• the transmissivity of light through an optical fiber is highly dependent on the properties of the coatings applied to the fiber.
• the coatings typically include a primary coating and a secondary coating, where the secondary coating surrounds the primary coating and the primary coating contacts the glass fiber (which includes a central glass core surrounded by a glass cladding).
• the secondary coating is a harder material (higher Young’s modulus) than the primary coating and is designed to protect the glass waveguide from damage caused by abrasion or external forces that arise during processing, handling, and installation of the fiber.
• the primary coating is a softer material (low Young’s modulus) and is designed to buffer or dissipates stresses that result from forces applied to the outer surface of the secondary coating.
• the primary coating is especially important in dissipating stresses that arise when the fiber is bent.
• the bending stresses transmitted to the glass waveguide on the fiber needs to be minimized because bending stresses create local perturbations in the refractive index profile of the glass waveguide.
• the local refractive index perturbations lead to intensity losses for the light transmitted through the waveguide.
• the primary coating minimizes bend-induced intensity losses. [0004] To minimize bending losses, it is desirable to develop primary coating materials with increasingly lower Young’s moduli. Coating materials with a Young’s modulus below 1 MPa are preferred.
• fiber stripping and splice operations require primary coatings with proper adhesion to the glass fiber. If the adhesion of the primary coating to the glass fiber is too strong, residue from the primary coating remains on the glass fiber and it is difficult to achieve a clean strip. A clean strip is needed to insert the glass fiber into a connector.
• the opening in fiber connectors is closely matched to the diameter of the glass fiber and the presence of coating residue on the glass fiber prevents insertion of the fiber into a connector.
• the adhesion requirements are particularly stringent for ribbons, which are linear fiber assemblies that include multiple fibers in a common matrix. When connecting ribbons, all fibers are stripped simultaneously and each fiber must be stripped cleanly without introducing defects in the coating remaining on the unstrapped portion of the glass fiber.
• the present disclosure provides primary coatings formed as cured products of curable compositions.
• the coatings feature low Young’s modulus, low pullout force and good cohesion. The variation in pullout force over time is low, indicating stable adhesion and consistent performance of the coating over time.
• the coatings can be used as primary coatings for optical fibers.
• the primary coatings can be stripped cleanly from glass fiber and are resistant to defect formation when subjected to stripping forces.
• the primary coatings can be applied to individual fibers or to each of multiple fibers in a ribbon.
• the curable compositions can also be used to form cured films and other cured products used in applications outside the field of optical fibers.
• a primary coating for optical fibers comprising:
• a cured product of a curable composition comprising:
• a pullout force less than 1.7 lb f /cm when configured as a primary coating with thickness 32.5 pm on a glass fiber having a diameter of 125 pm in an as-drawn state said fiber pullout force increasing by less than a factor of 2.0 upon aging said primary coating on said glass fiber for at least 60 days.
• An optical fiber comprising:
• said primary coating comprising:
• a cured product of a curable composition comprising:
• a pullout force less than 1.7 lbfcm when configured as a primary coating with thickness 32.5 pm on a glass fiber having a diameter of 125 pm in an as-drawn state said fiber pullout force increasing by less than a factor of 2.0 upon aging said primary coating on said glass fiber for at least 60 days.
• the present disclosure further includes fiber coatings and cured products formed from the oligomers or coating compositions described herein.
• the fiber coating features low Young’s modulus, low pullout force and small increases in pullout force with aging.
• the present disclosure further includes an optical fiber coated with a coating formed from a composition disclosed herein, wherein the optical fiber includes a glass waveguide and the coating surrounds and is in direct contact with the glass waveguide.
• FIG. 1 is a schematic view of a coated optical fiber according one embodiment.
• FIG. 2 is a schematic view of a representative optical fiber ribbon.
• the representative optical fiber ribbon includes twelve coated optical fibers.
• FIG. 3 shows force as a function of time in a pullout force test of a fiber sample.
• FIG. 4 shows variation in pullout force with time for a fiber sample.
• FIG. 5 shows variation in pullout force with time for a fiber sample.
• FIG. 6 shows variation in pullout force with time for a fiber sample.
• FIG. 7 shows variation in pullout force with time for a fiber sample.
• FIG. 8 shows variation in pullout force with time for a fiber sample.
• compositions and methods of the disclosure include those having any value or any combination of the values, specific values, more specific values, and preferred values described herein.
• indefinite article“a” or“an” and its corresponding definite article“the” as used herein means at least one, or one or more, unless specified otherwise.
• Curable coating compositions include one or more curable components.
• curable is intended to mean that the component, when exposed to a suitable source of curing energy, includes one or more curable functional groups capable of forming covalent bonds that participate in linking the component to itself or to other components of the coating composition.
• the product obtained by curing a curable coating composition is referred to herein as the cured product of the composition.
• the cured product is preferably a polymer.
• the curing process is induced by energy. Forms of energy include radiation or thermal energy ln a preferred embodiment, curing occurs with radiation. Curing induced by radiation is referred to herein as radiation curing or photocuring.
• a radiation-curable component is a component that can be induced to undergo a curing reaction when exposed to radiation of a suitable wavelength at a suitable intensity for a sufficient period of time. Suitable wavelengths include wavelengths in the infrared, visible, or ultraviolet portion of the electromagnetic spectrum. The radiation curing reaction preferably occurs in the presence of a photo initiator.
• a radiation-curable component may also be thermally curable.
• a thermally-curable component is a component that can be induced to undergo a curing reaction when exposed to thermal energy of sufficient intensity for a sufficient period of time.
• a thermally curable component may also be radiation curable.
• a curable component includes one or more curable functional groups.
• a curable component with only one curable functional group is referred to herein as a monofunctional curable component.
• a curable component having two or more curable functional groups is referred to herein as a multifunctional curable component.
• Multifunctional curable components include two or more functional groups capable of forming covalent bonds during the curing process and can introduce crosslinks into the polymeric network formed during the curing process. Multifunctional curable components may also be referred to herein as“crosslinkers” or “curable crosslinkers”. Curable components include curable monomers and curable oligomers. Examples of functional groups that participate in covalent bond formation during the curing process are identified hereinafter.
• molecular weight when applied to polyols means number average molecular weight.
• (meth)acrylate means methacrylate, acrylate, or a combination of methacrylate and acrylate.
• the present description relates to curable coating compositions, coatings formed from the curable coating compositions, and coated articles coated or encapsulated by the coating obtained by curing the curable coating compositions ln a preferred embodiment, the curable coating composition is a composition for forming coatings for optical fibers, the coating is an optical fiber coating, and the coated article is a coated optical fiber.
• the present description also relates to methods of making curable coating compositions, methods of forming coatings from the curable coating compositions, and methods of coating fibers with the curable coating
• Coatings formed from the curable coating compositions can be stripped cleanly from glass fiber and have strong cohesion.
• One embodiment relates to a coated optical fiber.
• An example of a coated optical fiber is shown in schematic cross-sectional view in FIG. 1.
• Coated optical fiber 10 includes a glass optical fiber 1 1 surrounded by primary coating 16 and secondary coating 18.
• the primary coating 16 is the cured product of a curable coating composition in accordance with the present description.
• the glass fiber 11 is an uncoated optical fiber including a core 12 and a cladding 14, as is familiar to the skilled artisan.
• Core 12 has a higher refractive index than cladding 14 and glass fiber 11 functions as a waveguide ln many applications, the core and cladding have a discernible core-cladding boundary.
• the core and cladding can lack a distinct boundary.
• One such fiber is a step-index fiber.
• Another such fiber is a graded-index fiber, which has a core whose refractive index varies with distance from the fiber center.
• a graded- index fiber is formed basically by diffusing the glass core and cladding layer into one another.
• the cladding can include one or more layers.
• the one or more cladding layers can include an inner cladding layer that surrounds the core and an outer cladding layer that surrounds the inner cladding layer.
• the inner cladding layer and outer cladding layer differ in refractive index.
• the inner cladding layer may have a lower refractive index than the outer cladding layer.
• a depressed index layer may also be positioned between the inner cladding layer and outer cladding layer.
• the optical fiber may also be single or multi-mode at the wavelength of interest, e.g.,
• the optical fiber may be adapted for use as a data transmission fiber (e.g. SMF-28 ® , LEAF ® , and METROCOR ® , each of which is available from Coming lncorporated of Coming, N. Y.)
• the optical fiber may perform an amplification, dispersion compensation, or polarization maintenance function.
• the coatings described herein are suitable for use with virtually any optical fiber for which protection from the environment is desired.
• the primary coating 16 preferably has a higher refractive index than the cladding of the optical fiber in order to allow it to strip errant optical signals away from the optical fiber core.
• the primary coating should maintain adequate adhesion to the glass fiber during thermal and hydrolytic aging, yet be strippable from the glass fiber for splicing purposes.
• the primary coating typically has a thickness in the range of 25-40 pm (e.g. about 32.5 pm).
• Primary coatings are typically formed by applying a curable coating composition to the glass fiber as a viscous liquid and curing.
• FIG. 2 illustrates an optical fiber ribbon 30.
• the ribbon 30 includes a plurality of optical fibers 20 and a matrix 32 encapsulating the plurality of optical fibers.
• Optical fibers 20 include a core glass region, a cladding glass region, a primary coating, and a secondary coating as described above.
• Optical fibers 20 may also include an ink layer.
• the secondary coating may include a pigment.
• the optical fibers 20 are aligned relative to one another in a substantially planar and parallel relationship.
• the optical fibers in fiber optic ribbons are encapsulated by the ribbon matrix 32 in any known configuration (e.g., edge-bonded ribbon, thin-encapsulated ribbon, thick-encapsulated ribbon, or multi-layer ribbon) by conventional methods of making fiber optic ribbons.
• the fiber optic ribbon 30 contains twelve (12) optical fibers 20; however, it should be apparent to those skilled in the art that any number of optical fibers 20 (e.g., two or more) may be employed to form fiber optic ribbon 30 disposed for a particular use.
• the ribbon matrix 32 can be formed from the same composition used to prepare a secondary coating, or the ribbon matrix 32 can be formed from a different composition that is otherwise compatible for use.
• the present disclosure provides a primary coating for optical fibers that exhibits low Young’s modulus, low pullout force, and strong cohesion.
• the present disclosure provides curable coating compositions that enable formation of a primary coating that features clean strippability and high resistance to defect formation during the stripping operation.
• Low pullout force facilitates clean stripping of the primary coating with minimal residue and strong cohesion inhibits initiation and propagation of defects in the primary coating when it is subjected to stripping forces.
• the primary coating is a cured product of a radiation-curable coating composition that includes an oligomer, a monomer, a photoinitiator and, optionally, an additive.
• the present disclosure describes oligomers for the radiation-curable coating compositions, radiation-curable coating compositions containing at least one of the oligomers, cured products of the radiation- curable coating compositions that include at least one of the oligomers, optical fibers coated with a radiation-curable coating composition containing at least one of the oligomers, and optical fibers coated with the cured product of a radiation- curable coating composition containing at least one of the oligomers.
• the oligomer includes a polyether urethane diacrylate compound and a di-adduct compound.
• the polyether urethane diacrylate compound has a linear molecular structure.
• the oligomer is formed from a reaction between a diisocyanate compound, a polyol compound, and a hydroxy acrylate compound, where the reaction produces a polyether urethane diacrylate compound as a primary product (majority product) and a di-adduct compound as a byproduct (minority product). The reaction forms a urethane linkage upon reaction of an isocyanate group of the diisocyanate compound and an alcohol group of the polyol.
• the hydroxy acrylate compound reacts to quench residual isocyanate groups that are present in the composition formed from reaction of the diisocyanate compound and polyol compound.
• quench refers to conversion of isocyanate groups through a chemical reaction with hydroxyl groups of the hydroxy acrylate compound. Quenching of residual isocyanate groups with a hydroxy acrylate compound converts terminal isocyanate groups to terminal acrylate groups.
• a preferred diisocyanate compound is represented by molecular formula (I): which includes two terminal isocyanate groups separated by a linkage group Ri.
• the linkage group Ri includes an alkyl ene group.
• the alkylene group of linkage group Ri is linear (e.g. methylene or ethylene), branched (e.g. isopropylene), or cyclic (e.g. cyclohexylene, phenylene).
• the cyclic group is aromatic or non-aromatic.
• the linkage group Ri is 4,4'-methylene bis(cyclohexyl) group and the diisocyanate compound is 4,4 '-methylene bis(cyclohexyl isocyanate). In some embodiments, the linkage group Ri lacks an aromatic group, or lacks a phenylene group, or lacks an oxyphenylene group.
• the polyol is represented by molecular formula (II): where R 2 includes an alkylene group, -O-R2- is a repeating alkoxylene group, and x is an integer.
• x is greater than 20, or greater than 40, or greater than 50, or greater than 75, or greater than 100, or greater than 125, or greater than 150, or in the range from 20 - 500, or in the range from 20 - 300, or in the range from 30 - 250, or in the range from 40 - 200, or in the range from 60 - 180, or in the range from 70 - 160, or in the range from 80 - 140.
• R 2 is preferably a linear or branched alkylene group, such as methylene, ethylene, propylene (normal, iso or a combination thereof), or butylene (normal, iso, secondary, tertiary, or a combination thereof).
• the polyol may be a polyalkylene oxide, such as polyethylene oxide, or a polyalkylene glycol, such as polypropylene glycol.
• Polypropylene glycol is a preferred polyol.
• the molecular weight of the polyol is greater than 1000 g/mol, or greater than 2500 g/mol, or greater than 5000 g/mol, or greater than 7500 g/mol, or greater than 10000 g/mol, or in the range from 1000 g/mol - 20000 g/mol, or in the range from 2000 g/mol - 15000 g/mol, or in the range from 2500 g/mol - 12500 g/mol, or in the range from 2500 g/mol - 10000 g/mol, or in the range from 3000 g/mol - 7500 g/mol, or in the range from 3000 g/mol - 6000 g/mol, or in the range from 3500 g/mol - 5500 g/mol.
• the unsaturation of the polyol is less than 0.25 meq/g, or less than 0.15 meq/g, or less than 0.10 meq/g, or less than 0.08 meq/g, or less than 0.06 meq/g, or less than 0.04 meq/g, or less than 0.02 meq/g, or less than 0.01 meq/g, or less than 0.005 meq/g, or in the range from 0.001 meq/g - 0.15 meq/g, or in the range from 0.005 meq/g - 0.10 meq/g, or in the range from 0.01 meq/g - 0.10 meq/g, or in the range from 0.01 meq/g - 0.05 meq/g, or in the range from 0.02 meq/g - 0.10 meq/g, or in the range from 0.02 meq/g - 0.05 meq/g.
• unsaturation refers to the value determined by the standard method reported in ASTM D4671-16.
• the polyol is reacted with mercuric acetate and methanol in a methanolic solution to produce acetoxymercuricmethoxy compounds and acetic acid.
• the reaction of the polyol with mercuric acetate is equimolar and the amount of acetic acid released is determined by titration with alcoholic potassium hydroxide to provide the measure of unsaturation used herein.
• sodium bromide is added to convert mercuric acetate to the bromide.
• the reaction to form the oligomer further includes addition of a hydroxy acrylate compound to react with terminal isocyanate groups present in unreacted starting materials (e.g. the diisocyanate compound) or products formed in the reaction of the diisocyanate compound with the polyol (e.g. urethane compounds with terminal isocyanate groups).
• the hydroxy acrylate compound reacts with terminal isocyanate groups to provide terminal acrylate groups for one or more constituents of the oligomer.
• the hydroxy acrylate compound is present in excess of the amount needed to fully convert terminal isocyanate groups to terminal acrylate groups.
• the oligomer includes a single polyether urethane acrylate compound or a combination of two or more polyether urethane acrylate compounds.
• the hydroxy acrylate compound is represented by molecular formula (III): where R3 includes an alkylene group.
• the alkylene group of R3 is linear (e.g. methylene or ethylene), branched (e.g. isopropylene), or cyclic (e.g. phenylene).
• the hydroxy acrylate compound includes substitution of the ethylenically unsaturated group of the acrylate group.
• Substituents of the ethylenically unsaturated group include alkyl groups.
• An example of a hydroxy acrylate compound with a substituted ethylenically unsaturated group is a hydroxy methacrylate compound.
• the discussion that follows describes hydroxy acrylate compounds. It should be understood, however, that the discussion applies to substituted hydroxy acrylate compounds and in particular to hydroxy methacrylate compounds.
• the hydroxy acrylate compound is a hydroxyalkyl acrylate, such as 2 -hydroxy ethyl acrylate.
• the hydroxy acrylate compound may include water at residual or higher levels. The presence of water in the hydroxy acrylate compound may facilitate reaction of isocyanate groups to reduce the concentration of unreacted isocyanate groups in the final reaction composition.
• the water content of the hydroxy acrylate compound is at least 300 ppm, or at least 600 ppm, or at least 1000 ppm, or at least 1500 ppm, or at least 2000 ppm, or at least 2500 ppm.
• the groups Ri, R 2 , and R 3 are all the same, are all different, or include two groups that are the same and one group that is different.
• the diisocyanate compound, hydroxy acrylate compound and polyol are combined simultaneously and reacted, or are combined sequentially (in any order) and reacted.
• the oligomer is formed by reacting a diisocyanate compound with a hydroxy acrylate compound and reacting the resulting product composition with a polyol.
• the oligomer is formed by reacting a diisocyanate compound with a polyol compound and reacting the resulting product composition with a hydroxy acrylate compound.
• the oligomer is formed from a reaction of a diisocyanate compound, a hydroxy acrylate compound, and a polyol, where the molar ratio of the diisocyanate compound to the hydroxy acrylate compound to the polyol in the reaction process is n:m:p.
• n, m, and p are referred to herein as mole numbers or molar proportions of diisocyanate, hydroxy acrylate, and polyol; respectively.
• the mole numbers n, m and p are positive integer or positive non- integer numbers.
• n is in the range from 3.0 - 5.0, or in the range from 3.0 - 4.5, or in the range from 3.2 - 4.8, or in the range from 3.4 - 4.6, or in the range from 3.6 - 4.4
• m is in the range from l.50n - 3 to 2.50n - 5, or in the range from l.55n - 3 to 2.45n - 5, or in the range from l.60n - 3 to 2.40n - 5, or in the range from l.65n - 3 to 2.35n - 5.
• n:m:p scales proportionally.
• the mole number m may be selected to provide an amount of the hydroxy acrylate compound to stoichiometrically react with unreacted isocyanate groups present in the product composition formed from the reaction of diisocyanate compound and polyol used to form the oligomer.
• the isocyanate groups may be present in unreacted diisocyanate compound
• the mole number m may be selected to provide an amount of the hydroxy acrylate compound in excess of the amount needed to stoichiometrically react with any unreacted isocyanate groups present in the product composition formed from reaction of the diisocyanate compound and the polyol.
• the hydroxy acrylate compound is added as a single aliquot or multiple aliquots.
• an initial aliquot of hydroxy acrylate is included in the reaction mixture used to form the oligomer and the product composition formed can be tested for the presence of unreacted isocyanate groups (e.g. using FTIR spectroscopy to detect the presence of isocyanate groups). Additional aliquots of hydroxy acrylate compound may be added to the product composition to
• stoichiometrically react with unreacted isocyanate groups using, for example, FTIR spectroscopy to monitor a decrease in a characteristic isocyanate frequency (e.g. at 2260 cm 1 - 2270 cm 1 ) as isocyanate groups are converted by the hydroxy acrylate compound).
• a characteristic isocyanate frequency e.g. at 2260 cm 1 - 2270 cm 1
• aliquots of hydroxy acrylate compound in excess of the amount needed to stoichiometrically react with unreacted isocyanate groups are added.
• the ratio of the mole number m to the mole number n influences the relative proportions of polyether urethane diacrylate compound and di-adduct compound in the oligomer and differences in the relative proportions of polyether urethane diacrylate compound and di-adduct compound lead to differences in the tear strength and/or critical stress of coatings formed from the oligomer.
• the oligomer is formed from a reaction mixture that includes 4,4'- methylene bis(cyclohexyl isocyanate), 2-hydroxyethyl acrylate, and polypropylene glycol in the molar ratios n:m:p as specified above, where the polypropylene glycol has a number average molecular weight in the range from 2500 g/mol - 6500 g/mol, or in the range from 3000 g/mol - 6000 g/mol, or in the range from 3500 g/mol - 5500 g/mol.
• the oligomer includes two components.
• the first component is a polyether urethane diacrylate compound having the molecular formula (IV):
• the second component is a di-adduct compound having the molecular formula (V): where the groups Ri, R 2 , R 3 , and the integer x are as described hereinabove, y is a positive integer, and it is understood that the group Ri in molecular formulas (IV) and (V) is the same as group Ri in molecular formula (I), the group R 2 in molecular formula (IV) is the same as group R 2 in molecular formula (II), and the group R 3 in molecular formulas (IV) and (V) is the same as group R 3 in molecular formula (III).
• the di-adduct compound corresponds to the compound formed by reaction of both terminal isocyanate groups of the diisocyanate compound of molecular formula (I) with the hydroxy acrylate compound of molecular formula (III) where the diisocyanate compound has undergone no reaction with the polyol of molecular formula (II).
• the di-adduct compound is formed from a reaction of the diisocyanate compound with the hydroxy acrylate compound during the reaction used to form the oligomer.
• the di-adduct compound is formed independent of the reaction used to form the oligomer and is added to the product of the reaction used to form the polyether urethane diacrylate compound or to a purified form of the polyether urethane diacrylate compound.
• the hydroxy group of the hydroxy acrylate compound reacts with an isocyanate group of the diisocyanate compound to provide a terminal acrylate group. The reaction occurs at each isocyanate group of the diisocyanate compound to form the di-adduct compound.
• the di-adduct compound is present in the oligomer in an amount of at least 1.0 wt%, or at least 1.5 wt%, or at least 2.0 wt%, or at least 2.25 wt%, or at least 2.5 wt%, or at least 3.0 wt%, or at least 3.5 wt%, or at least 4.0 wt%, or at least 4.5 wt%, or at least 5.0 wt%, or at least 7.0 wt % or at least 9.0 wt%, or in the range from 1.0 wt% - 10.0 wt%, or in the range from 2.0 wt% - 9.0 wt%, or in the range from 2.5 wt% - 6.0 wt%, or in the range from 3.0 wt% - 8.0 wt%, or in the range from 3.0 wt% to 5.0 wt%, or in the range from 3.0 wt% - 5.5 wt%, or in
• An illustrative reaction for synthesizing an oligomer in accordance with the present disclosure includes reaction of a diisocyanate compound (4,4 '-methylene bis(cyclohexyl isocyanate, which is also referred to herein as H12MDI) and a polyol (polypropylene glycol with M n ⁇ 4000 g/mol, which is also referred to herein as PPG4000) to form a poly ether urethane diisocyanate compound with formula (VI):
• ⁇ PPG4000 ⁇ refer to residues of H12MDI and PPG4000 remaining after the reaction.
• the polyether urethane diisocyanate compound has a repeat unit of the type ⁇ (Hl2MDI ⁇ PPG4000) ⁇ .
• the particular polyether urethane diisocyanate shown includes two PPG4000 units.
• the reaction may also provide products having one PPG4000 unit, or three or more PPG4000 units.
• the polyether urethane diisocyanate and any unreacted H12MDI include terminal isocyanate groups.
• a hydroxy acrylate compound such as 2 -hydro xyethyl acrylate, which is referred to herein as HEA
• HEA hydroxy acrylate compound
• the conversion of terminal isocyanate groups to terminal acrylate groups effects a quenching of the isocyanate group.
• the amount of HEA included in the reaction may be an amount estimated to react stoichiometrically with the expected concentration of unreacted isocyanate groups or an amount in excess of the expected stoichiometric amount.
• Reaction of HEA with the polyether urethane diisocyanate compound forms the poly ether urethane acrylate compound with formula (VII):
• oligomer in accordance with the present disclosure. As described more fully hereinbelow, when one or more oligomers are used in coating
• compositions, coatings having improved tear strength and critical stress characteristics result.
• oligomers having a high proportion of di-adduct compound provide coatings with high tear strengths and/or high critical stress values.
• the foregoing reaction may be generalized to an arbitrary combination of a diisocyanate compound, a hydroxy acrylate compound, and a polyol, where the hydroxy acrylate compound reacts with terminal isocyanate groups to form terminal acrylate groups and where urethane linkages form from reactions of isocyanate groups and alcohol groups of the polyol or hydroxy acrylate compound.
• the oligomer includes a compound that is a polyether urethane diacrylate compound with formula (X):
• y is the same as y in formula (IV) and is 1, or 2, or 3 or 4 or higher; and x is determined by the number of repeat units of the polyol (as described hereinabove).
• y is 1, or 2, or 3, or 4 or higher; and x is determined by the number of repeat units of the polyol (as described hereinabove).
• the reaction between the diisocyanate compound, hydroxy acrylate compound, and polyol yields a series of polyether urethane diacrylate compounds that differ in y such that the average value of y over the distribution of compounds present in the final reaction mixture is a non-integer.
• the average value of y in the polyether urethane diisocyanates and polyether urethane diacrylates of molecular formulas (VI) and (IV) corresponds to p or p-l (where p is as defined hereinabove).
• the average number of occurrences of the group Ri in the polyether urethane diisocyanates and polyether urethane diacrylates of the molecular formulas (XII) and (IV) correspond to n (where n is as defined hereinabove).
• the relative proportions of the polyether urethane diacrylate and di-adduct compounds produced in the reaction are controlled by varying the molar ratio of the mole numbers n, m, and p.
• Variations in the mole numbers n, m, and p provide control over the relative proportions of polyether urethane diacrylate and di-adduct formed in the reaction.
• Increasing the mole number n relative to the mole number m or the mole number p may increase the amount of di-adduct compound formed in the reaction.
• Variations in the relative proportions of di-adduct and polyether urethane diacrylate are obtained through changes in the mole numbers n, m, and p and through such variations, it is possible to precisely control the tear strength, critical stress, tensile toughness, and other mechanical properties of coatings formed from coating compositions that include the oligomer.
• control of tear strength, tensile toughness, and other mechanical properties is achieved by varying the proportions polyether urethane diacrylate compound and di-adduct compound.
• oligomers having variable proportions of di-adduct compound can be prepared.
• the variability in proportion of di-adduct compound can be finely controlled to provide oligomers based on a polyether urethane diacrylate compound with a fixed number of polyol units that provide coatings that offer precise or targeted values of tear strength, critical stress, tensile toughness, or other mechanical properties.
• a coating composition that incorporates an oligomer that includes a polyether urethane acrylate compound represented by molecular formula (IV) and a di-adduct compound represented by molecular formula (V), where concentration of the di-adduct compound in the oligomer is at least 1.0 wt%, or at least 1.5 wt%, or at least 2.0 wt%, or at least 2.25 wt%, or at least 2.5 wt%, or at least 3.0 wt%, or at least 3.5 wt%, or at least 4.0 wt%, or at least 4.5 wt%, or at least 5.0 wt%, or at least 7.0 wt % or at least 9.0 wt%, or in the range from 1.0 wt% - 10.0 wt%, or in the range from 2.0 wt% to 9.0 wt%, or in the range from 3.0 wt% to 8.0 wt%
• concentration of di-adduct is expressed in terms of wt% of the oligomer and not in terms of wt% in the coating composition.
• concentration of the di-adduct compound is increased in one embodiment by varying the molar ratio n:m:p of diisocyanate:hydroxy acrylate:polyol.
• molar ratios n:m:p that are rich in diisocyanate relative to polyol promote the formation of the di-adduct compound.
• the amount of hydroxy acrylate can also be increased.
• p polyol
• n (diisocyanate) and m (hydroxy acrylate) are p + 1 and 2, respectively.
• the available hydroxy acrylate reacts with isocyanate groups present on the oligomer or free diisocyanate molecules to form terminal acrylate groups.
• the relative kinetics of the two reaction pathways dictates the relative amounts of polyether urethane diacrylate and di-adduct compounds formed and the deficit in hydroxy acrylate relative to the amount required to quench all unreacted isocyanate groups may be controlled to further influence the relative proportions of polyether urethane diacrylate and di-adduct formed in the reaction.
• the reaction includes heating the reaction composition formed from the diisocyanate compound, hydroxy acrylate compound, and polyol.
• the heating facilitates conversion of terminal isocyanate groups to terminal acrylate groups through a reaction of the hydroxy acrylate compound with terminal isocyanate groups.
• the hydroxy acrylate compound is present in excess in the initial reaction mixture and/or is otherwise available or added in unreacted form to effect conversion of terminal isocyanate groups to terminal acrylate groups.
• the heating occurs at a temperature above 40 °C for at least 12 hours, or at a temperature above 40 °C for at least 18 hours, or at a temperature above 40 °C for at least 24 hours, or at a temperature above 50 °C for at least 12 hours, or at a temperature above 50 °C for at least 18 hours, or at a temperature above 50 °C for at least 24 hours, or at a temperature above 60 °C for at least 12 hours, or at a temperature above 60 °C for at least 18 hours, or at a temperature above 60 °C for at least 24 hours.
• terminal isocyanate groups on the polyether urethane diacrylate compound or starting diisocyanate compound is facilitated by the addition of a supplemental amount of hydroxy acrylate compound to the reaction mixture.
• a supplemental amount of hydroxy acrylate compound may deviate from the theoretical number of equivalents due, for example, to incomplete reaction or a desire to control the relative proportions of polyether urethane diacrylate compound and di adduct compound.
• reaction has proceeded to completion or other endpoint, it is preferable to quench (neutralize) residual isocyanate groups to provide a stabilized reaction product.
• supplemental hydroxy acrylate is added to accomplish this objective.
• the amount of supplemental hydroxy acrylate compound is in addition to the amount included in the initial reaction process.
• the presence of terminal isocyanate groups at any stage of the reaction is monitored, for example, by FTIR spectroscopy (e.g. using a characteristic isocyanate stretching mode near 2265 cm 1 ) and supplemental hydroxy acrylate compound is added as needed until the intensity of the characteristic stretching mode of isocyanate groups is negligible or below a pre-determined threshold.
• supplemental hydroxy acrylate compound is added beyond the amount needed to fully convert terminal isocyanate groups to terminal acrylate groups.
• supplemental hydroxy acrylate compound is included in the initial reaction mixture (as an amount above the theoretical amount expected from the molar amounts of diisocyanate and polyol), added as the reaction progresses, and/or added after reaction of the diisocyanate and polyol compounds has occurred to completion or pre-determined extent. [0072] Amounts of hydroxy acrylate compound above the amount needed to fully convert isocyanate groups are referred to herein as excess amounts of hydroxy acrylate compound.
• the excess amount of hydroxy acrylate compound is at least 20% of the amount of supplemental hydroxy acrylate compound needed to fully convert terminal isocyanate groups to terminal acrylate groups, or at least 40% of the amount of supplemental hydroxy acrylate compound needed to fully convert terminal isocyanate groups to terminal acrylate groups, or at least 60% of the amount of supplemental hydroxy acrylate compound needed to fully convert terminal isocyanate groups to terminal acrylate groups, or at least 90% of the amount of supplemental hydroxy acrylate compound needed to fully convert terminal isocyanate groups to terminal acrylate groups.
• the amount of supplemental hydroxy acrylate compound may be sufficient to completely or nearly completely quench residual isocyanate groups present in the oligomer formed in the reaction. Quenching of isocyanate groups is desirable because isocyanate groups are relatively unstable and often undergo reaction over time. Such reaction alters the characteristics of the reaction composition or oligomer and may lead to inconsistencies in coatings formed therefrom. Reaction compositions and products formed from the starting diisocyanate and polyol compounds that are free of residual isocyanate groups are expected to have greater stability and predictability of characteristics.
• the oligomer of the coating composition includes a polyether urethane diacrylate compound and di-adduct compound as described hereinabove ln some aspects, the oligomer includes two or more polyether urethane diacrylate compounds and/or two or more di-adduct compounds.
• the oligomer content of the coating composition includes the combined amounts of the one or more polyether urethane diacrylate compound(s) and one or more di-adduct compound(s) and is greater than 20 wt%, or greater than 30 wt%, or greater than 40 wt%, or in the range from 20 wt% - 80 wt%, or in the range from 30 wt% - 70 wt%, or in the range from 40 wt% - 60 wt%, where the concentration of di-adduct compound within the oligomer content is as described above.
• the curable coating composition further includes one or more monomers.
• the one or more monomers is/are selected to be compatible with the oligomer, to control the viscosity of the coating composition to facilitate processing, and/or to influence the physical or chemical properties of the coating formed as the cured product of the coating composition.
• the monomers include ethylenically-unsaturated compounds, ethoxylated acrylates, ethoxylated alkylphenol monoacrylates, propylene oxide acrylates, n-propylene oxide acrylates, isopropylene oxide acrylates, monof mctional acrylates, monof mctional aliphatic epoxy acrylates, multifunctional acrylates, multifunctional aliphatic epoxy acrylates, and combinations thereof.
• Representative radiation-curable ethylenically unsaturated monomers include alkoxylated monomers with one or more acrylate or methacrylate groups.
• An alkoxylated monomer is one that includes one or more alkoxylene groups, where an alkoxylene group has the form -O-R- and R is a linear or branched alkylene group.
• alkoxylene groups include ethoxylene (- O-CH2-CH2-), n-propoxylene (-O-CH2-CH2-CH2-), isopropoxylene (-O-CFb-CF ⁇ CFF)-, or -O- CH(CH3)-CH2-), etc.
• the degree of alkoxylation refers to the number of alkoxylene groups in the monomer. In one embodiment, the alkoxylene groups are bonded consecutively in the monomer.
• monomers include ethylenically unsaturated monomers such as lauryl acrylate (e.g., SR335 available from Sartomer Company, Inc., AGEFLEX FA12 available from BASF, and PFIOTOMER 4812 available from IGM Resins), ethoxylated nonylphenol acrylate (e.g., SR504 available from Sartomer Company, Inc.
• lauryl acrylate e.g., SR335 available from Sartomer Company, Inc.
• AGEFLEX FA12 available from BASF
• PFIOTOMER 4812 available from IGM Resins
• ethoxylated nonylphenol acrylate e.g., SR504 available from Sartomer Company, Inc.
• caprolactone acrylate e.g., SR495 available from Sartomer Company, Inc., and TONE M-100 available from Dow Chemical
• phenoxyethyl acrylate e.g., SR339 available from Sartomer Company, Inc., AGEFLEX PEA available from BASF
• PFIOTOMER 4035 available from IGM Resins
• isooctyl acrylate e.g., SR440 available from Sartomer Company, Inc.
• tridecyl acrylate e.g., SR489 available from Sartomer Company, Inc.
• isobomyl acrylate e.g., SR506 available from Sartomer Company, Inc. and AGEFLEX IBOA available from CPS Chemical Co.
• tetrahydrofurfuryl acrylate e.g., SR285 available from Sartomer Company, Inc.
• stearyl acrylate e.g., SR257 available from Sartomer Company, Inc.
• isodecyl acrylate e.g., SR395 available from Sartomer Company, Inc.
• AGEFLEX FA10 available from BASF
• 2-(2- ethoxyethoxy) ethyl acrylate e.g., SR256 available from Sartomer Company, Inc.
• epoxy acrylate e.g., CN120, available from Sartomer Company, and EBECRYL 3201 and 3604, available from Cytec Industries Inc.
• lauryloxyglycidyl acrylate e.g., CN130 available from Sartomer Company
• phenoxyglycidyl acrylate e.g., CN131 available from Sartomer Company
• the monomer component of the coating composition includes a multifunctional (meth)acrylate.
• Multifunctional ethylenically unsaturated monomers include multifunctional acrylate monomers and multifunctional methacrylate monomers.
• Multifunctional acrylates are acrylates having two or more polymerizable acrylate moieties per molecule, or three or more polymerizable acrylate moieties per molecule. Examples of multifunctional
• (meth)acrylates include dipentaerythritol monohydroxy pentaacrylate (e.g., PHOTOMER 4399 available from IGM Resins); methylolpropane polyacrylates with and without alkoxylation such as trimethylolpropane triacrylate, ditrimethylolpropane tetraacrylate (e.g., PHOTOMER 4355, IGM Resins); alkoxylated glyceryl triacrylates such as propoxylated glyceryl triacrylate with propoxylation being 3 or greater (e.g., PHOTOMER 4096, IGM Resins); and erythritol polyacrylates with and without alkoxylation, such as pentaerythritol tetraacrylate (e.g., SR295, available from Sartomer Company, Inc.
• PHOTOMER 4399 available from IGM Resins
• methylolpropane polyacrylates with and without alkoxylation such as trimethylo
• ethoxylated pentaerythritol tetraacrylate e.g., SR494, Sartomer Company, Inc.
• dipentaerythritol pentaacrylate e.g., PHOTOMER 4399, IGM Resins, and SR399, Sartomer Company, Inc.
• tripropyleneglycol diacrylate propoxylated hexanediol diacrylate, tetrapropyleneglycol diacrylate
• the coating composition includes an N-vinyl amide monomer such as an N-vinyl lactam, or N-vinyl pyrrolidinone, or N-vinyl caprolactam, where the N-vinyl amide monomer is present in the coating composition at a concentration greater than 1.0 wt%, or greater than 2.0 wt%, or greater than 3.0 wt%, or in the range from 1.0 wt% - 15.0 wt%, or in the range from 2.0 wt% - 10.0 wt%, or in the range from 3.0 wt% - 8.0 wt%.
• an N-vinyl amide monomer such as an N-vinyl lactam, or N-vinyl pyrrolidinone, or N-vinyl caprolactam
• the coating composition includes one or more mono functional acrylate or methacrylate monomers in an amount from 5 - 95 wt%, or from 30 - 75 wt%, or from 40 - 65 wt%.
• the coating composition may include one or more monofunctional aliphatic epoxy acrylate or methacrylate monomers in an amount from 5 - 40 wt%, or from 10 - 30 wt%.
• the monomer component of the coating composition includes a hydro xyf mctional monomer.
• a hydroxyfimctional monomer is a monomer that has a pendant hydroxy moiety in addition to other reactive functionality such as (meth)acrylate.
• hydroxyfimctional monomers including pendant hydroxyl groups include caprolactone acrylate (available from Dow Chemical as TONE M-100); poly(alkylene glycol) mono(meth)acrylates, such as polyethylene glycol) monoacrylate, polypropylene glycol) monoacrylate, and poly(tetramethylene glycol) monoacrylate (each available from Monomer, Polymer & Dajac Labs); 2-hydroxy ethyl (meth)acrylate, 3-hydroxypropyl (meth) acrylate, and 4-hydro xybutyl (meth)acrylate (each available from Aldrich).
• caprolactone acrylate available from Dow Chemical as TONE M-100
• poly(alkylene glycol) mono(meth)acrylates such as polyethylene glycol) monoacrylate, polypropylene glycol) monoacrylate, and poly(tetramethylene glycol) monoacrylate (each available from Monomer, Polymer & Dajac Labs)
• the hydroxyfimctional monomer is present in an amount sufficient to improve adhesion of the coating to the optical fiber.
• the hydroxyfimctional monomer is present in the coating composition in an amount between about 0.1 wt% and about 25 wt%, or in an amount between about 5 wt% and about 8 wt%.
• the use of the hydroxyfimctional monomer may decrease the amount of adhesion promoter necessary for adequate adhesion of the primary coating to the optical fiber.
• the use of the hydroxyfimctional monomer may also tend to increase the hydrophilicity of the coating. Hydroxyfimctional monomers are described in more detail in U.S. patent No. 6,563,996, the disclosure of which is hereby incorporated by reference in its entirety.
• the total monomer content of the coating composition is between about 5 wt% and about 95 wt%, or between about 30 wt% and about 75 wt%, or between about 40 wt% and about 65 wt%.
• the coating composition may also include one or more polymerization initiators and one or more additives.
• the polymerization initiator facilitates initiation of the polymerization process associated with the curing of the coating composition to form the coating.
• Polymerization initiators include thermal initiators, chemical initiators, electron beam initiators, and photoinitiators.
• Photoinitiators are preferred polymerization initiators. Photoinitiators include ketonic photo initiating additives and/or phosphine oxide additives. When used in the formation reaction of the coating of the present disclosure, the photoinitiator is present in an amount sufficient to enable rapid radiation curing.
• the wavelength of curing radiation is infrared, visible, or ultraviolet. Representative wavelengths include wavelengths in the range from 300 nm - 1000 nm, or in the range from 300 nm - 700 nm, or in the range from 300 nm - 400 nm, or in the range from 325 nm - 450 nm, or in the range from 325 nm - 400 nm, or in the range from 350 nm - 400 nm. Curing can be accomplished with a lamp source (e.g. Hg lamp) or LED source (e.g. a UVLED, visible LED, or infrared LED).
• a lamp source e.g. Hg lamp
• LED source
• Representative photoinitiators include l-hydroxycyclohexylphenyl ketone (e.g.,
• IRGACURE 184 available from BASF
• bis(2,6-dimethoxybenzoyl)-2,4,4- trimethylpentylphosphine oxide e.g., commercial blends IRGACURE 1800, 1850, and 1700 available from BASF
• 2,2-dimethoxy-2-phenylacetophenone e.g., IRGACURE 651, available from BASF
• bis(2,4,6-trimethylbenzoyl)-phenylphosphine oxide IRGACURE 819
• (2,4,6- trimethylbenzoyl)diphenyl phosphine oxide (LUCIRIN TPO, available from BASF (Munich, Germany)
• ethoxy(2,4,6-trimethylbenzoyl)-phenylphosphine oxide ethoxy(2,4,6-trimethylbenzoyl)-phenylphosphine oxide (LUCIRIN TPO-L from BASF); and combinations thereof.
• the coating composition includes a single photoinitiator or a combination of two or more photoinitiators.
• the total photoinitiator concentration in the coating composition is greater than 0.25 wt%, or greater than 0.50 wt%, or greater than 0.75 wt%, or greater than 1.0 wt%, or in the range from 0.25 wt% - 5.0 wt%, or in the range from 0.50 wt% - 4.0 wt%, or in the range from 0.75 wt% - 3.0 wt%.
• the coating composition optionally includes one or more additives.
• Additives include an adhesion promoter, a strength additive, an antioxidant, a catalyst, a stabilizer, an optical brightener, a property enhancing additive, an amine synergist, a wax, a lubricant, and/or a slip agent.
• Some additives operate to control the polymerization process, thereby affecting the physical properties (e.g., modulus, glass transition temperature) of the polymerization product formed from the coating composition.
• Other additives affect the integrity of the cured product of the coating composition (e.g., protect against de-polymerization or oxidative degradation).
• An adhesion promoter is a compound that facilitates adhesion of the primary coating and/or primary composition to glass (e.g. the cladding portion of a glass fiber).
• Suitable adhesion promoters include alkoxysilanes, mercapto -functional silanes, organotitanates, and zirconates.
• adhesion promoters include mercaptoalkyl silanes or mercaptoalkoxy silanes such as 3-mercaptopropyl-trialkoxysilane (e.g., 3-mercaptopropyl-trimethoxysilane, available from Gelest (Tullytown, Pa.)); bis(trialkoxysilyl-ethyl)benzene; acryloxypropyltrialkoxysilane (e.g., (3-acryloxypropyl)-trimethoxysilane, available from Gelest), methacryloxypropyltrialkoxysilane, vinyltrialkoxysilane, bis(trialkoxysilylethyl)hexane, allyltrialkoxysilane, styrylethyltrialkoxysilane, and bis(trimethoxysilylethyl)benzene (available from United Chemical Technologies (Bristol, Pa.)); see U.S. Patent No. 6,316,
• the adhesion promoter is present in the coating composition in an amount between 0.02 wt% and 10.0 wt%, or between 0.05 wt% and 4.0 wt%, or between 0.1 wt% and 4.0 wt%, or between 0.1 wt% and 3.0 wt%, or between 0.1 wt% and 2.0 wt%, or between O.l wt% and 1.0 wt%, or between 0.5 wt% and 4.0 wt%, or between 0.5 wt% and 3.0 wt%, or between 0.5 wt% and 2.0 wt%, or between 0.5 wt% to 1.0 wt%.
• a representative antioxidant is thiodiethylene bis[3-(3,5-di-tert-butyl)-4-hydroxy-phenyl) propionate] (e.g., IRGANOX 1035, available from BASF).
• an antioxidant is present in the coating composition in an amount greater than 0.25 wt%, or greater than 0.50 wt%, or greater than 0.75 wt%, or greater than 1.0 wt%, or an amount in the range from 0.25 wt% - 3.0 wt%, or an amount in the range from 0.50 wt% - 2.0 wt%, or an amount in the range from 0.75 wt% - 1.5 wt%.
• optical brighteners include TIN OPAL OB (available from BASF);
• Blankophor KLA available from Bayer
• bisbenzoxazole compounds phenylcoumarin compounds
• bis(styryl)biphenyl compounds are present in the coating composition at a concentration of 0.005 wt% - 0.3 wt%.
• Representative amine synergists include triethanolamine; l,4-diazabicyclo[2.2.2]octane (DABCO), triethylamine, and methyldiethanolamine.
• DABCO l,4-diazabicyclo[2.2.2]octane
• an amine synergist is present at a concentration of 0.02 wt% - 0.5 wt%.
• Curing of the coating composition provides a cured product, such as a primary coating, with increased resistance to defect formation during manufacturing or subsequent processing, including splicing.
• the present disclosure demonstrates that primary coatings having low pullout force and strong cohesion can be stripped cleanly from glass fibers while maintaining resistance to defect formation during splicing.
• the primary coatings of the present disclosure combine a low Young’s modulus with strong cohesion to enable splicing of fibers and ribbons with minimal coating residue on the spliced portion of the optical fiber and few defects in the coating remaining on the unspliced portion of the optical fiber.
• a glass fiber is drawn from a heated preform and sized to a target diameter (typically 125 pm). The glass fiber is then cooled and directed to a coating system that applies a liquid primary coating composition to the glass fiber.
• a coating system that applies a liquid primary coating composition to the glass fiber.
• Two process options are viable after application of the liquid primary coating composition to the glass fiber. In one process option (wet-on-dry process), the liquid primary coating composition is cured to form a solidified primary coating, the liquid secondary coating composition is applied to the cured primary coating, and the liquid secondary coating composition is cured to form a solidified secondary coating.
• the liquid secondary coating composition is applied to the liquid primary coating composition, and both liquid coating compositions are cured simultaneously to provide solidified primary and secondary coatings.
• the coating system further applies a tertiary coating to the secondary coating.
• the tertiary coating is an ink layer used to mark the fiber for identification purposes.
• the fiber is collected and stored at room temperature. Collection of the fiber typically entails winding the fiber on a spool and storing the spool.
• the coating compositions disclosed herein are compatible with fiber draw processes that operate at a draw speed greater than 35 m/s, or greater than 40 m/s, or greater than 45 m/s, or greater than 50 m/s, or greater than 55 m/s.
• pullout force is a reliable indicator of the adhesion of a primary coating to a glass fiber.
• Adhesion of the primary coating to a glass fiber needs to be strong enough to prevent separation of the primary coating from the glass fiber during routine handling, but not so strong that it is difficult to remove the primary coating during the stripping and splicing operations.
• the primary coatings disclosed herein exhibit a pullout force consistent with the level of adhesion needed for adherence to a glass fiber while permitting removal without residue during stripping.
• the pullout force of primary coatings evolves over time.
• the pullout force increases from an initial value at the time of draw to higher values at later times. Time evolution of pullout force is undesirable.
• adhesion of the primary coating to the glass fiber becomes stronger and it becomes more difficult to remove the primary coating during splicing without leaving residue on the stripped portion of the fiber.
• the pullout force of the primary coatings disclosed herein exhibits improved stability over time relative to prior art primary coatings.
• stability over time is measured beginning from the time the fiber is stored after coating in the manufacturing process used to make the fiber from a preform.
• the state of the optical fiber at the initial time of storage in the original manufacturing process is referred herein as the“as- drawn state” of the optical fiber ln the as-drawn state, the fiber is coated and at room temperature on a storage device (e.g. spool) positioned along a continuous process pathway extending from the preform through a coating system to the storage device.
• the time of placement of the fiber in the as-drawn state is the time at which the fiber is collected at the storage device.
• Measurements of the properties of the fiber in the as-drawn state are made as soon as practicable following time of collection at the storage device ln instances in which a measurement delay occurs, the properties of the fiber in the as-drawn state can be determined from data obtained at later times through back extrapolation of a fit obtained from Eq. (3) given below.
• Cohesion refers to tear strength and/or tensile toughness.
• Tensile toughness is a measure of the force needed to initiate a break in a coating and tear strength is a measure of the force required to expand a break in a coating once it has been initiated.
• the present disclosure extends to optical fibers coated with the cured product of the coating compositions.
• the optical fiber includes a glass waveguide with a higher index glass core region surrounded by a lower index glass cladding region.
• a coating formed as a cured product of the present coating compositions surrounds and is in direct contact with the glass cladding.
• the cured product of the present coating compositions preferably functions as the primary coating of the fiber.
• the fiber may include a secondary coating or both a secondary and tertiary coating.
• Coating Compositions The components of coating compositions and the
• Coating composition C is a comparative composition. Additional commercial coating compositions designated as D, E, F, and G were tested for comparative purposes. The commercial compositions were obtained from DSM Desotech (Elgin, IL) and included conventional oligomers. The specific formulations are proprietary to the vendor. Composition D had product code 950-076, Composition E had product code 950-030, Composition G had product code 3741-143, and Composition F was a variant of Composition G that included an adhesion promoter. The oligomers present in comparative coating compositions C-G contained a lower concentration of di-adduct compound than coating compositions A and B.
• Oligomer 1 and Oligomer 2 are products of reactions of H12MDI (4,4'-methylene bis(cyclohexyl isocyanate), PPG4000 (polypropylene glycol with M n ⁇ 4000 g/mol) and HEA (2-hydroxyethyl acrylate). The reaction conditions are described below. SR504 is
• NVC N-vinylcaprolactam (available from ISP Technologies).
• TPO is (2, ⁇ 4, 6-trimethylbenzoyl) diphenyl phosphine oxide (available from BASF under the trade name Lucirin) and functions as a photo initiator.
• Irganox 1035 is thio diethylene bis[3-(3,5-di-tert-butyl)-4-hydroxy-phenyl) propionate] (available from BASF under the trade name Irganox 1035) and functions as an antioxidant.
• 3-acryloxypropyl trimethoxysilane available from Gelest
• 3-mercaptopropyl trimethoxysilane available from Aldrich
• Tetrathiol is pentaerythritoltetrakis(3-mercaptopropionate) (available from Aldrich) and functions as a quencher of residual dibutyltin dilaurate catalyst that may be present in Oligomer 1 and Oligomer 2.
• Coating compositions A and B are curable coating compositions that included an oligomer of the type disclosed herein.
• preparation of exemplary oligomers from FH2MDI (4,4 '-methylene bis(cyclohexyl isocyanate), PPG4000 (polypropylene glycol with M n ⁇ 4000 g/mol) and HEA (2-hydroxyethyl acrylate) in accordance with the reaction scheme disclosed hereinabove is described. All reagents were used as supplied by the manufacturer and were not subjected to further purification.
• H12MDI was obtained from ALDRICH.
• PPG4000 was obtained from COVESTRO and was certified to have an unsaturation of 0.004 meq/g as determined by the method described in the standard ASTM D4671-16.
• HEA was obtained from KOWA.
• dibutyltin dilaurate was used as a catalyst (at a level of 160 ppm based on the mass of the initial reaction mixture) and 2,6-di-tert-butyl-4-methylphenol (BHT) was used as an inhibitor (at a level of 400 ppm based on the mass of the initial reaction mixture).
• Oligomer 1 and Oligomer 2 were prepared by mixing 4,4’-methylene bis(cyclohexyl isocyanate), dibutyltin dilaurate and 2,6-di-/e/7-butyl-4 methylphenol at room temperature in a 500 mL flask.
• the 500 mL flask was equipped with a thermometer, a CaCf drying tube, and a stirrer. While continuously stirring the contents of the flask, PPG4000 was added over a time period of 30-40 minutes using an addition funnel. The internal temperature of the reaction mixture was monitored as the PPG4000 was added and the introduction of PPG4000 was controlled to prevent excess heating (arising from the exothermic nature of the reaction).
• the reaction mixture was heated in an oil bath at about 70°C - 75°C for about 1 - 1 1 ⁇ 2 hours. At various intervals, samples of the reaction mixture were retrieved for analysis by infrared spectroscopy (FT1R) to monitor the progress of the reaction by determining the concentration of unreacted isocyanate groups. The concentration of unreacted isocyanate groups was assessed based on the intensity of a characteristic isocyanate stretching mode near 2265 cm 1 . The flask was removed from the oil bath and its contents were allowed to cool to below 65 °C. Addition of supplemental HEA was conducted to insure complete quenching of isocyanate groups. The supplemental HEA was added dropwise over 2-5 minutes using an addition funnel.
• F1R infrared spectroscopy
• the flask was returned to the oil bath and its contents were again heated to about 70°C - 75°C for about 1 - 1 1 ⁇ 2 hours.
• FTIR analysis was conducted on the reaction mixture to assess the presence of isocyanate groups and the process was repeated until enough supplemental HEA was added to fully react any unreacted isocyanate groups. The reaction was deemed complete when no appreciable isocyanate stretching intensity was detected in the FTIR measurement.
• the FIEA amounts listed in Table 1 include the initial amount of FIEA in the composition and any amount of supplemental FIEA needed to quench unreacted isocyanate groups.
• the concentration (wt%) of di-adduct compound was determined by gel permeation chromatography (GPC).
• GPC gel permeation chromatography
• a Waters Alliance 2690 GPC instrument was used to determine the di adduct concentration.
• the mobile phase was THF.
• the columns were calibrated with polystyrene standards ranging from 162 - 6,980,000 g/mol using EasiCal PS-l & 2 polymer calibrant kits (Agilent Technologies Part Nos. PL2010-505 and PL2010-0601).
• the detector was a Waters Alliance 2410 differential refractometer operated at 40 °C and sensitivity level 4. The samples were injected twice along with a THF + 0.05% toluene blank.
• Standard solutions with di-adduct concentrations of 115.2 pg/g, 462.6 pg/g, 825.1 pg/g, and 4180 pg/g were prepared.
• the dimension“pg/g” refers to pg of di-adduct per gram of total solution (di-adduct + THF)).
• Two 100 pL aliquots of each di-adduct standard solution were injected into the column to obtain the calibration curve.
• the retention time of the di-adduct was approximately 23 min and the area of the GPC peak of the di-adduct was measured and correlated with di-adduct concentration.
• the di-adduct concentration in Oligomer 1 and Oligomer 2 was determined using the calibration. Samples were prepared by diluting -0.10 g of each oligomer in THF to obtain a -1.5 g test solution. The test solution was run through the GPC instrument and the area of the peak associated with the di-adduct compound was determined. The di-adduct concentration in units of Lig/g was obtained from the peak area and the calibration curve, and was converted to wt% by multiplying by the weight (g) of the test solution and dividing by the weight of the sample of oligomer before dilution with THF. The wt% of di-adduct compound present in Oligomer 1 and Oligomer 2 are reported in Table 3. The entries in Table 1 for Oligomer 1 and Oligomer 2 include the combined amount of polyether urethane acrylate compound and di-adduct compound.
• the illustrative oligomers include a polyether urethane compound of the type shown in molecular formula (IV) hereinabove and an enhanced concentration of di-adduct compound of the type shown in molecular formula (V) hereinabove.
• coatings formed using oligomers that contain the di-adduct compound in amounts of at least 2.50 wt% have significantly improved pullout force, tear strength and/or tensile toughness (relative to coatings formed from polyether urethane acrylate compounds alone or polyether urethane acrylate compounds combined with lesser amounts of di-adduct compound) while maintaining a favorable Young’s modulus for primary coatings of optical fibers.
• Oligomer 3 is a commercial oligomer (obtained from Dymax (product code BR3741). Oligomer 3 was prepared from starting materials similar to those used for Oligomer 1 and Oligomer 2. The ratio n:m:p used in the preparation of Oligomer 3, however, produced a smaller concentration of di-adduct compound.
• Young’s Modulus and Tensile Toughness were measured on films formed by the curing coating compositions A, B, and C. Separate films were formed from each coating composition. Wet films of the coating composition were cast on silicone release paper with the aid of a draw-down box having a gap thickness of about 0.005". The wet films were cured with a U V dose of 1.2 J/cm 2 (measured over a wavelength range of 225 - 424 nm by a Light Bug model IL490 from International Light) by a Fusion Systems UV curing apparatus with a 600 W/in D-bulb (50% Power and approximately 12 ft/min belt speed) to yield cured coatings in film form. Cured film thickness was between about 0.0030" and 0.0035".
• the films were aged (23° C, 50% relative humidity) for at least 16 hours prior to testing. Film samples were cut to dimensions of 12.5 cm x 13 mm using a cutting template and a scalpel. Young's modulus, tensile strength at break, and % elongation (% strain at break) were measured at room temperature (approximately 20 °C) on the film samples using a MTS Sintech tensile test instrument following procedures set forth in ASTM Standard D882-97. Young’s modulus is defined as the steepest slope of the beginning of the stress-strain curve. Tensile toughness is defined as the integrated area under the stress-strain curve. Films were tested at an elongation rate of 2.5 cm/min with the initial gauge length of 5.1 cm.
• Tear Strength Tear strength of films formed from coating compositions A - C was measured. Tear strength (G c ) is related to the force required to break the coating when the coating is under tension. The tear strength is calculated from Eq. (1):
• F break is the force at break
• b is the slit length
• d is the film thickness
• B is the width of the test piece.
• S is the segment modulus calculated from the stresses at elongations of 0.05% and 2%
• C is a sample geometry factor defined as follows for the technique used herein to determine tear strength:
• Tear strength (G c ) was measured at room temperature (approximately 20 °C) with a MTS Sintech tensile tester. Each coating composition measured was cast on a glass plate with the aid of a draw-down box having a gap thickness of about 0.005" and immediately cured under UV irradiation using a dose of 1 J/cm 2 .
• the shape and dimensions of the cured films were prepared according to the International Standard ISO 816 (second edition 1983-12-01) “Determination of tear strength of small test pieces (Delft test pieces)”. The cured films were conditioned at 23°C ⁇ 2°C and 50% relative humidity (RH) for at least 16 hours.
• the initial gauge length was 5.0 cm and test speed was set at 0.1 mm/m in. Three to five specimens of each film were tested. Tear strength (G c ) was calculated from Eqs. (1) and (2).
• slit length b was 5.0 mm
• width B of the test piece was 9.0 mm
• sample geometry factor C was 1.247.
• Pullout force was measured at room temperature (approximately 20 °C) on samples of glass fibers coated with each of the coating compositions A-G. Separate glass fibers (diameter 125 pm) were coated with each of the coating compositions A-G. The coating compositions were cured with mercury lamps to form primary coatings on the glass fiber. The thickness of the primary coating was 32.5 pm. The primary coating surrounded and was in direct contact with the glass fiber. The fiber samples also included a secondary coating with a thickness of 26 pm and a Young’s modulus of 1600 MPa. The secondary coatings were formed by applying a secondary coating composition to the (cured) primary coating and curing the secondary coating composition with mercury lamps to form a secondary coating. The secondary coating surrounded and was in direct contact with the primary coating.
• the pullout force test measures the peak force needed to pull a 1 cm length of glass fiber out of a surrounding coating.
• the coating at each end of the coated fiber was fixed (glued) to separate support surfaces made with a 1 square inch tab of heavy stock paper.
• the one end of the fiber sample was cut at a distance of 1 cm from the support surface and nicked at the interface with the support surface.
• the glass fiber was then pulled out of the coating by pulling the two tabs apart and the peak force was determined.
• the peak force is a measure of the strength of adhesion of the coating to the glass fiber. Additional details of the test procedure follow.
• Pullout force measurements were made on fiber samples with a length of five inches. Each end of the fiber sample was glued to a 1" x 1" paper tab (heavy stock, comparable to a manila folder). Each end of the fiber sample was oriented perpendicular to an edge of a paper tab and a strip of glue extending a distance of 0.625 inches from the center of the edge toward the center of the tab was applied. The fiber sample was placed on the glue with a portion of the fiber extending slightly beyond the glue. The glue was allowed to dry (about 30 min). The fiber sample was then conditioned in a controlled environment (room temperature and -50% relative humidity) for at least two hours.
• a controlled environment room temperature and -50% relative humidity
• a gauge length (1 cm) was defined by cutting the coating at one end of the fiber sample at a position 1 cm from the edge of the tab. The cut extended through the fiber and glue to the tab. The fiber sample was then turned over and the coating of the cut end of the fiber sample was nicked at the edge of the tab. After nicking, the fiber sample was oriented vertically and the tabs were inserted into upper and lower pneumatic grips of a universal tensile machine equipped with a 5 lb load cell (Instron instrument). The tab with the nicked end of the fiber was inserted into the upper grip. The grips were closed and pulled apart at a rate of 5 mm/min until the glass fiber was separated from the coating (approximately two minutes). The force applied was measured as a function of time and recorded to provide a force curve (force as a function of time). Pullout force was defined to be the peak force observed during the pullout test. The pullout force measurements were completed at room temperature.
• a representative schematic force curve is shown in FIG. 3.
• the force was observed to initially increase with time to a peak value and then decreased.
• the pullout force is the peak force.
• the decrease in force following the peak force is associated with the frictional force of sliding the coating along the glass fiber.
• the contact area of the coating with the fiber decreases and a commensurate decrease in force is observed.
• the force drops to zero.
• the Young’s modulus (E) of the present coatings have a Young’s modulus (E) of less than 1.0 MPa, or less than 0.8 MPa, or less than 0.7 MPa, or less than 0.6 MPa, or less than 0.5 MPa, or in the range from 0.1 MPa - 1.0 MPa, or in the range from 0.3 MPa - 1.0 MPa, or in the range from 0.45 MPa - 1.0 MPa, or in the range from 0.2 MPa - 0.9 MPa, or in the range from 0.3 MPa - 0.8 MPa, where Young’s modulus (E) is determined according to the procedure described herein.
• the tear strength (G c ) of the present coatings is at least 30 J/m 2 , or at least 35 J/m 2 , or at least 40 J/m 2 , or at least 45 J/m 2 , or at least 50 J/m 2 , or at least 55 J/m 2 , or in the range from 30 J/m 2 - 70 J/m 2 , or in the range from 35 J/m 2 - 65 J/m 2 , or in the range from 40 J/m 2 - 60 J/m 2 , where tear strength (G c ) is determined according to the procedure described herein.
• the tensile toughness of the present coatings is greater than 500 kJ/m 3 , or greater than 600 kJ/m 3 , or greater than 700 kJ/m 3 , or greater than 800 kJ/m 3 , or in the range from 500 kJ/m 3 to 1200 kJ/m 3 , or in the range from 600 kJ/m 3 to 1100 kJ/m 3 , or in the range from 700 kJ/m 3 to 1000 kJ/m 3 , where tensile toughness is determined according to the procedure described herein.
• coatings or cured products prepared from a coating composition that includes an oligomer in accordance with the present disclosure have a Young’s modulus of less than 1.0 MPa with a tear strength of at least 35 J/m 2 , or a Young’s modulus of less than 0.8 MPa with a tear strength of at least 35 J/m 2 , or a Young’s modulus of less than 0.6 MPa with a tear strength of at least 35 J/m 2 , or a Young’s modulus of less than 0.5 MPa with a tear strength of at least 35 J/m 2 , or a Young’s modulus of less than 1.0 MPa with a tear strength of at least 45 J/m 2 , or a Young’s modulus of less than 0.8 MPa with a tear strength of at least 45 J/m 2 , or a Young’s modulus of less than 0.6 MPa with a tear strength of at least 45 J/m 2 , or a Young’s modulus of less than less than 0.6 MPa with
• coatings or cured products prepared from a coating composition that includes an oligomer in accordance with the present disclosure have a Young’s modulus in the range from 0.1 MPa - 1.0 MPa with a tear strength in the range from 35 J/m 2 - 75 J/m 2 , or a Young’s modulus in the range from 0.45 MPa - 1.0 MPa with a tear strength in the range from 35 J/m 2 - 75 J/m 2 , or a Young’s modulus in the range from 0.3 MPa - 0.8 MPa with a tear strength in the range from 35 J/m 2 - 75 J/m 2 , or a Young’s modulus in the range from 0.1 MPa - 1.0 MPa with a tear strength in the range from 45 J/m 2 - 70 J/m 2 , or a Young’s modulus in the range from 0.45 MPa - 1.0 MPa with a tear strength in the range from 45 J/m 2 - 70 J/m 2 , or a
• FIGS. 4-8 show the time dependence of the pullout force at room temperature
• FIGS. 4 and 5 indicate that coating compositions A and B provide primary coatings for fiber samples with both a low pullout force in the as-drawn state and a small increase in pullout force over time as the fiber sample ages.
• the low pullout force in the as- drawn state indicates that adhesion of the primary coating to the glass fiber is adequate to retain the coating on the glass fiber while permitting removal of the coating without leaving residue during a stripping operation.
• the small increase in pullout force over time indicates that the adhesion properties remain stable and that the coating can be cleanly removed from the fiber over extended periods of time.
• the coating derived from comparative coating composition C exhibits a low pullout force for fiber samples in the as-drawn state, but a large increase in pullout force as the fiber sample ages (FIG. 6).
• the large increase in pullout force over time indicates a greater tendency for residue to remain on the fiber during stripping if the fiber is stored for an extended period of time before the stripping operation.
• Coatings derived from comparative coating compositions D-G show small increases in pullout force over time as the fiber sample ages, but exhibit large pullout forces for fiber samples in the as-drawn state (FIGS. 7-8).
• the large pullout force in the as-drawn state indicates that the fiber cannot be cleanly stripped and the increase in pullout force over time indicates that the problem becomes more severe over time.
• a primary coating can be stripped cleanly from a glass fiber if the pullout force of a primary coating is less than 1.7 lb f /cm when the fiber is in the as-drawn state and the pullout force increases by less than a factor of 2.0 at room temperature over a time period of 60 or more days beginning from the time the fiber is placed in the as-drawn state, where pullout force is determined according to the procedure described herein.
• the pullout force of the primary coatings disclosed herein is less than 1.7 lb f /cm when the fiber is in the as-drawn state and increases by less than a factor of 2.0 over a time period of 60 or more days beginning from the time the fiber is placed in the as-drawn state. In another aspect, the pullout force of the primary coatings disclosed herein is less than 1.7 lb f /cm when the fiber is in the as-drawn state and increases by less than a factor of 1.9 over a time period of 60 or more days beginning from the time the fiber is placed in the as-drawn state.
• the pullout force of the primary coatings disclosed herein is less than 1.7 lb f /cm when the fiber is in the as-drawn state and increases by less than a factor of 1.8 over a time period of 60 or more days beginning from the time the fiber is placed in the as-drawn state.
• pullout force is determined according to the procedure described herein.
• the pullout force of the primary coatings disclosed herein is less than 1.5 lb f /cm when the fiber is in the as-drawn state and increases by less than a factor of 2.0 over a time period of 60 or more days beginning from the time the fiber is placed in the as-drawn state. In another aspect, the pullout force of the primary coatings disclosed herein is less than 1.5 lb f /cm when the fiber is in the as-drawn state and increases by less than a factor of 1.9 over a time period of 60 or more days beginning from the time the fiber is placed in the as-drawn state.
• the pullout force of the primary coatings disclosed herein is less than 1.5 lb f /cm when the fiber is in the as-drawn state and increases by less than a factor of 1.8 over a time period of 60 or more days beginning from the time the fiber is placed in the as-drawn state.
• pullout force is determined according to the procedure described herein.
• the pullout force of the primary coatings disclosed herein is less than 1.3 lb f /cm when the fiber is in the as-drawn state and increases by less than a factor of 2.0 over a time period of 60 or more days beginning from the time the fiber is placed in the as-drawn state. In another aspect, the pullout force of the primary coatings disclosed herein is less than 1.3 lb f /cm when the fiber is in the as-drawn state and increases by less than a factor of 1.9 over a time period of 60 or more days beginning from the time the fiber is placed in the as-drawn state.
• the pullout force of the primary coatings disclosed herein is less than 1.3 lb f /cm when the fiber is in the as-drawn state and increases by less than a factor of 1.8 over a time period of 60 or more days beginning from the time the fiber is placed in the as-drawn state.
• pullout force is determined according to the procedure described herein.
• the pullout force of the primary coatings disclosed herein is less than 1.1 lb f /cm when the fiber is in the as-drawn state and increases by less than a factor of 2.0 over a time period of 60 or more days beginning from the time the fiber is placed in the as-drawn state. In another aspect, the pullout force of the primary coatings disclosed herein is less than 1.1 lb f /cm when the fiber is in the as-drawn state and increases by less than a factor of 1.9 over a time period of 60 or more days beginning from the time the fiber is placed in the as-drawn state.
• the pullout force of the primary coatings disclosed herein is less than 1.1 lb f /cm when the fiber is in the as-drawn state and increases by less than a factor of 1.8 over a time period of 60 or more days beginning from the time the fiber is placed in the as-drawn state.
• pullout force is determined according to the procedure described herein.
• the pullout force of the present coatings when configured as a primary coating with a thickness of 32.5 pm on a glass fiber having a diameter of 125 pm and surrounded by a secondary coating with a thickness of 26 pm and Young’s modulus of 1600 MPa in the as-drawn state, is less than 1.8 lb f , or less than 1.6 lb f , or less than 1.5 lb f , or less than 1.4 lb f , or less than 1.3 lb f , or in the range from 1.2 lb f to 1.8 lb f , or in the range from 1.3 lb f to 1.7 lb f , or in the range from 1.4 lb f to 1.6 lb f , where pullout force is determined according to the procedure described herein.
• a coating for optical fibers comprising:
• Clause 6 of the description discloses: The coating of any of clauses 1-5, wherein said pullout force increases by less than a factor of 1.9 upon aging said coating on said glass fiber for at least 60 days.
• polyol compound having unsaturation less than 0.1 meq/g
• diisocyanate compound, said hydroxy (meth)acrylate compound and said polyol compound are present in said composition in the molar ratio n:m:p, respectively, where n is in the range from 3.0 to 5.0, m is in the range from l.50n - 3 to 2.50n - 5, and p is 2.
• Clause 15 of the description discloses: The coating of clause 14, wherein said diisocyanate compound comprises a compound having the formula: wherein the group Ri comprises an alkylene group.
• group R 2 comprises an alkylene group and x is between 40 and 100.
• an oligomer comprising:
• Ri, R 2 and R3 are independently selected from linear alkylene groups, branched alkylene groups, or cyclic alkylene groups; y is 1, 2, 3, or 4; x is between 40 and 100; said di-adduct compound is present in an amount of at least 1.0 wt%.
• An optical fiber comprising:

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